Summary

Catheterization of Intestinal Loops in Ruminants

Published: June 11, 2009
doi:

Summary

We describe a novel surgical method for catheterizing ‘intestinal loops’ within the ileum of sheep. Once animals have recovered from surgery and have cleared antibiotics and analgesics, multiple treatments can be deposited directly in loops via the catheters.

Abstract

The intestine is a complex structure that is involved not only in absorption of nutrients, but also acts as a barrier between the individual and the outside world. As such, the intestine plays a pivotal role in immunosurveillance and protection from enteric pathogens. Investigating intestinal physiology and immunology commonly employs ‘intestinal loops’ as an experimental model. The majority of these loop models are non-recovery surgical procedures that study short-term (<24 hr) changes in the intestine (1-3). We previously created a recovery intestinal loop model to specifically measure long-term (<6 mo) immunological changes in the intestine of sheep following exposure to vaccines, adjuvants, and viruses (4). This procedure localized treatments to a specific ‘loop’, allowing us to sample this area of the intestine. A significant drawback of this method is the single window of opportunity to administer treatments (i.e. at the time of surgery). Furthermore, samples of both the intestinal mucosa and luminal contents can only be taken at the termination of the project. Other salient limitations of the above model are that the surgical manipulation and requisite post-operative measures (e.g. administration of antibiotics and analgesics) can directly affect the treatment itself and/or alter immune function, thereby confounding results. Therefore, we modified our intestinal loop model by inserting long-term catheters into the loops. Sheep recover fully from the procedure, and are unaffected by the exteriorized catheters. Notably, the establishment of catheters in loops allows us to introduce multiple treatments over an extended interval, following recovery from surgery and clearance of drugs administered during surgery and the post-operative period.

Protocol

Experimental procedure:

  1. All instruments are autoclaved; non-autoclaveable materials are sterilized in Germex cold sterilization solution for a minimum of 10 min.
  2. Sheep are pre-medicated with acepromazine (0.05 mg/kg), glycopyrrolate (0.005 mg/kg), and butorphanol tartrate (0.2 mg/kg) IM, and left for 15-20 min.
  3. The neck is shaved and the skin surgically scrubbed. Once the jugular vein is visualized, 0.1 ml of lidocaine is injected SC over the vein, the catheter is introduced into the vein and secured to the skin using livestock identification tag cement and 2″ hospital tape. During surgery, the animals are given 10 ml/kg/hr of Plasmalyte 148 (by gravity flow).
  4. Diazepam (0.2 mg/kg) is administered IV, and anesthesia is induced with thiopental sodium (10 mg/kg). Lidocaine endotracheal spray is applied to the vocal folds, the sheep is intubated, and maintained on isoflurane (1.5-2.5% in 100% O2 at a rate of 4 L/min) for the duration of the surgery.
  5. The animal is placed in dorsal recumbency on a heated mat to help maintain body temperature during surgery. A stomach tube is inserted into the rumen to prevent excessive tympany.
  6. The ventral abdomen is shaved and the skin is prepared for surgery with three Prepodyne surgical scrubs. The abdomen is then draped, ensuring that appropriate exposure of the surgical site (umbilicus to caudal abdomen) is maintained.
  7. A 15-20 cm midline incision is made using an electroscapel, caudally from the umbilicus, and the ileocecal fold is located in the right lower quadrant of the abdomen. The caudal ileum and cecum are then exteriorized. Throughout the procedure, handling of the intestine is minimized and care is taken to ensure the exteriorized intestine is kept moist with warm (37-39°C) sterile phosphate buffered saline (PBS; pH 7.2).
  8. An 85 cm segment of ileum (i.e. the ‘intestinal segment’) is measured and then clamped with Doyen forceps (intestinal clamps) and large Kelly forceps at each end of the segment. Within the intestinal segment, ‘loops’ and ‘interspaces’ between the loops will be established. Doyen forceps are placed on the side of the ileum to be joined (anastomosis), and the Kelly forceps are placed on the intestinal segment side of the ileum.
  9. The ileum is cut between each Doyen and Kelly forcep and the intestinal segment designated for loops is gently flushed twice with 60 ml of warm PBS to remove ingesta.
  10. A cocktail of broad-spectrum antibiotics (200 mg enrofloxacin and 250 mg metronidazole in warm PBS, 60 ml total volume) is distributed throughout the intestinal segment and left for 30 min.
  11. The proximal and distal cut ends of the ileum (excluding the intestinal segment) are joined to form a continuous and functional intestinal tract. First, the ileum is aligned by two stay sutures, placed at the mesenteric and antimesenteric borders of the intestine, respectively. Then, a simple continuous suture pattern (2-0 Vicryl) is completed on both sides of the intestine to join the intestine together.
  12. Warm PBS (3-5 ml) is injected at the anastomosis site to check for leakage and suture failure. Then, the tip of Kelly forcep is pressed against the serosal surface of the intestine, close to the site of the anastomosis site, and advanced inwards at the anastomosis site to ensure the intestinal lumen is large and patent.
  13. The antibiotic cocktail is removed from the intestinal segment. Each end of the segment is closed with a simple continuous suture pattern (absorbable suture; 2-0 Vicryl) followed by an inverting suture pattern using 2-0 Vicryl.
  14. The 85 cm-long intestinal segment is partitioned into three 15 cm ‘loops’, two 15 cm-long ‘interspaces’ between the loops, and two 5 cm-long blunt-end compartments at the termini of the intestinal segment (Figure 1). The loops are created by placing a ligature around the intestine using 2-0 silk. It is noteworthy that major mesenteric vessels are not ligated during this procedure, as these are needed to supply the intestine with blood, maintaining intestinal viability. Also, the ligatures are left long, as they will be used to secure the catheters.
  15. Catheters (i.e. silastic tubing) are individually identified using a permanent marker. A silicon ball (5 mm-diameter) encircling the catheter, is placed 4-5 cm from the catheter end to help prevent the catheter from sliding out of the intestine (Figure 1). After sterilization by autoclaving, a non-antibiotic ointment (Orbeseal) is aseptically inserted into the catheter end (3-5 mm); this ensures that the catheter remains patent (i.e. it does not become plugged by sloughed mucosa within the loop).
  16. A small incision is placed at the cranial aspect of each of the three loops. Each hole is enlarged with a catheter introducer (i.e. ‘vessel dilator’), and a 6-8 cm segment of catheter is inserted caudally into the loop, until the silcone ball passes into the lumen (Figure 1).
  17. The intestinal wall is secured around the catheter with a purse string suture (2-0 Vicryl). The catheter is further secured to the intestine by tying the catheter with the ligature silk that delineated the cranial end of the loop.
  18. Ampicillin (5 ml; 100 mg/ml in warm PBS) is injected into each loop and interspace, and the intestine is placed back in the abdominal cavity. Cefazolin (8 ml; 100 mg/ml in warm PBS) is injected into the peritoneal cavity through the abdominal incision.
  19. A single small stab incision is made through the abdominal wall adjacent to the midline incision, and the catheters are exteriorized through this site.
  20. The position and tension of the catheters is adjusted within the peritoneal cavity. Abdominal muscles are closed with a simple interrupted suture pattern (absorbable suture; Catgut #3), and skin is closed with an interrupted horizontal mattress pattern (non-absorbable suture; Supramid #1).
  21. A curved hollow stainless steel tube (7 mm ID; 10 mm OD; 65 cm in length) is inserted under the skin near the abdominal incision, tunneled under the skin to an exit site just caudal to the neck and between the shoulders. The catheters are inserted into the tube and pushed forward for at least 50% of the tube length. The tube with the catheters is then pulled from the skin at the exit site, exposing the catheters.
  22. The tension of the catheters is adjusted at the stab incision site, and the skin is closed with Supramid #1.
  23. Individual catheters are identified and placed within a bandage “pouch” which is sutured to the skin with Supramid #1. The pouch protects the catheters from subsequent damage.
  24. Post-operatively, sheep are injected IM with flunixin (s.i.d.) at an initial dose 2.2 mg/kg, followed by a maintenance dose of 1.1 mg/kg s.i.d. for 3 days. Sheep also are injected IM with Hemostam (3 ml) and enrofloxacin (2.5 mg/kg) s.i.d. for 3 and 5 days, respectively. Animals are maintained on intravenous Plasmalyte 148 with 5% dextrose solution, administered continuously with a peristaltic pump to ensure that flow (145 ml/hr) continues regardless of body position. They are allowed to drink ad libitum, but feed is restricted until normal rumen and bowel functions are restored. Food intake, water consumption, body temperature, passage of feces and urine, gut noises, abdominal discomfort, demeanor, and blood glucose concentrations are closely monitored (b.i.d.); when necessary, glucose concentrations in the intravenous fluids are adjusted to maintain blood glucose concentrations within the normal range. Blood chemistry and hematology (i.e. albumin, alkaline phosphatase, alanine aminotransferase, amylase, calcium, cholesterol, creatinine, glucose, inorganic phosphate, total bilirubin, total protein, urea, globulin, sodium, potassium, chloride, partial pressure oxygen, pH, partial pressure carbon dioxide, bicarbonate, and total carbon dioxide, red and white blood cell counts, hematocrit, hemoglobin, differential white blood cell count and platelet count) are monitored before and immediately after surgery, and every other day thereafter. Once normal bowel function commences, intravenous fluid therapy is terminated and animals are transferred to paddocks (i.e. 5-7 days post-surgery). Animals are maintained in individual pens (within sight of other animals), thereby reducing stress and the chance of sustaining damage to their catheter pouches (e.g. chewing by a penmate).
  25. To inject treatments into individual loops, 5 ml of the treatment is injected into the catheter using a sterile syringe fitted with an 18 gauge, blunt-ended needle. To ensure the deposition of all of the treatment into the loop, the catheter is then injected with 3 ml of PBS.

Critical points:

Procedures of crucial importance to the success of this surgical procedure include: (1) verifying that the intestine is not twisted on itself before establishing the anastomosis; (2) ensuring the integrity and patency of the anastomosis; (3) adequately securing the catheter to the loop wall with the ligature delineating the cranial end of the loop, but ensuring that the attachment does not affect the patency of the catheter; (4) minimizing intestinal handling and ensuring that exteriorized intestine is kept moist; (5) ensuring the appropriate catheter tension; (6) ensuring that the integrity of the catheter is not affected during muscle and skin suturing; (7) preventing gorging by sheep post-surgery (i.e. during the period of post-operative ileus) which can cause ruminal impaction and impairment of rumen function; and (8) ensuring that animals receive sufficient intravenous fluid therapy for the first 3-5 days post-surgery, that blood glucose concentrations are carefully monitored, and glucose concentrations in the intravenous fluids are adjusted if necessary to prevent hypoglycemia.

figure 1
Figure 1. A schematic representation of catheterized ileal loops. Note the three 15 cm-long catheterized ‘loops’, the two 15 cm-long non-catheterized ‘interspaces’ established between the loops, and the two 5 cm-long terminal segments, all established within an 85 cm-long ‘intestinal segment’ of a sheep ileum.

Discussion

In this procedure, we were able to successfully establish catheters in intestinal loops established within the ileum of sheep. By adhering to stringent post-operative care, animals rapidly recovered from the procedure and resumed normal activity 5-7 days after surgery. We determined that the establishment of catheters within loops does not affect intestinal mucosal or immune function (data not shown) and animals can live for at least 8 wk after surgery. This procedure allows us to introduce multiple treatments into distinct immunological compartments over an extended interval, once animals have recovered from surgery, and to empirically measure the physiological and immunological effects of these treatments.

An important consideration for future experiments is the location of the intestinal segment within the small intestine. In this procedure we surgically created the intestinal segment within the ‘immunologically functional ileum’ as often defined by ileal (continuous) Peyer’s patches (5,6). This area can extend cranially up to 2 m beyond ileocecal fold. Although this region is considered anatomically as the jejunum, in the context of immunological function, it is ileum, highlighting the importance of considering function when describing intestinal regions.

Disclosures

The authors have nothing to disclose.

Acknowledgements

The research could not have been completed without the dedication and efforts of many persons at the Agriculture and Agri-Food Canada Research Centre, Lethbridge, Alberta, Canada. In that regard, we thank: Tara Shelton for pre- and post-operative care of animals, surgical preparation, and anesthesiology, analysis of samples, and assistance with video imaging; Randy Wilde and Estela Costa for pre- and post-operative care; Jenny Gusse for sample analysis; Byron Lee for the trocar image; and Brian Egland for sheep husbandry. We also thank Brent Selinger (Department of Biological Sciences, University of Lethbridge) for providing video equipment and advice, as well as other assistance (i.e. executive production), and the Curriculum Re-Development Centre, University of Lethbridge for videography expertise. This study was supported in part by grants from the Advanced Foods and Materials Network (G.D.I.), the Canada-Alberta Beef Industry Development Fund (G.D.I.), and Agriculture and Agri-Food Canada (G.D.I. and J.P.K.).

Materials

Category / Item NumberCompanyCatalogue
Surgeon supplies
Surgical glovesWDDCa103091
Surgical maskWDDCMAX53013
Surgical gownCDMVb3365
OB ApronWDDC900062
Surgical capWDDC903271
EZ Scrub brushWDDCBDC377479
Anesthesia and drugs
Anesthetic machineBoyle
SodasorbWDDC108638
LaryngoscopeWDDC
Laryngoscope blade (Miller blade #4)WDDC902667
Endotracheal tube (7.0 – 8.5 mm)WDDC
Lidocaine endotracheal sprayWDDC103364
AcepromazineWDDCAUS01020
GlycopyrrolateWDDCSAB2880
Butorphanol tartrateWDDCAYE304541
DiazepamWDDCsab790
Thiopental sodiumWDDC103508
Epinephrine hydrochlorideWDDC103856
DoxapramStrathcona Pharmacy
IsofluraneWDDC100339
HemostamWDDC103857
FlunixinWDDCsch140100
EnrofloxacinWDDChll0049
MetronidazoleWDDC101653
AmpicillinWDDCNOV67185-6
CefazolinWDDCnov69397
Surgical equipment and supplies
ElectroscapelMacanMV8
Heating matKanePHMD-48
Stomach tube (Nalgene tubing 5/16″ ID)Fisher Scientific
Needle driverWDDC108338
Addison brown forcepWDDC911075
Rat tooth forcepCDMV5275
Kelly forcepWDDC901133
Mosquito hemostatWDDC108471
Carmalt forcepWDDC901225
Scalpel handleWDDC900285
Scalpel blade #22WDDC900511
Metzenbaum scissorWDDC901166
Sharp-sharp scissorWDDC108264
Towel clampWDDC901213
Allis tissue forcepWDDC901201
Doyen’s forcepWDDC904226
Stainless steel bowlWDDC903601
Stainless steel trocar (curved)Local supplier
Catheter introducerWDDC11440
Surgical towelCDMV7972
Disposable drapeWDDC900035
Steri drapeCDMV2323
Drape (40 x 40 cm)CDMV8358
Surgical drape (7″ x 11 ¼” opening)CDMV2694
Vicryl (2-0)WDDCJJMJ333H
Silk 2-0WDDC105248
Catgut #3WDDCCSL547-2070
Supramid #1WDDCCSL547-3040
Needles (cutting and non-cutting)WDDC
Catheter
Silastic tubing (0.040″ ID, 0.085″ OD)Fisher Scientific11-189-15D
Orbeseal ointmentWDDC106344
Clear silicone (732 multi-purpose sealant)Local supplier
Blunt end needleWDDC905035
Marker (permanent industrial)Local supplier
Catheter pouch (constructed of Elastoplast 7.5 cm)WDDC104094
Bandages
Hospital tape (2″)WDDC103842
Hospital tape (1″)WDDCVLMRENF20
Gauze sponge 4×4WDDC107551
Gauze clingWDDC107633
Elastoplast 7.5cmWDDC104094
Elastoplast rippable bandageWDDC104093
Needles and syringes
Syringe (60 ml)WDDC104004
Syringe (10 ml)WDDCbdc301604
25G NeedleWDDCBDC305122
20G NeedleWDDCBDC305175
18G NeedleWDDC903353
Intravenous
Intracath IV catheter (16G 8″)WDDCbdc3831621
IV administration set (10 drop)WDDC101797
0.9% NaCl solutionWDDCBAXJB1322P
Plasmalyte 148 solutionWDDCBAXJB2534
DextroseWDDCMCT60190
Peristaltic pumpCole Parmer7524-10
Livestock identification tag cementLocal supplier
Sanatizers / disinfectants
Germex solutionWDDCmtc60270
Isopropyl alcoholWDDC104590
Stanhexidine cleanserWDDC109248
Prepodyne solutionWDDC105710
Prepodyne scrubWDDC105711

aWestern Drug Distribution Center LTD, Edmonton, AB.

bThe Veterinary Medication Distribution Center Inc., St. Hyacinthe, QE.

References

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  2. Santos, R. L., Zhang, S., Tsolis, R. M., Baumler, A. J., Adams, L. G. Morphologic and molecular characterization of Salmonella typhimurium infection in neonatal calves. Vet. Pathol. 39, 200-215 (2002).
  3. Uzzau, S., Leori, G. S., Petruzzi, V., Watson, P. R., Schianchi, G., Bacciu, D., Mazzarello, V., Wallis, T. S., Rubino, S. Salmonella enterica serovar-host specificity does not correlate with the magnitude of intestinal invasion in sheep. Infect. Immun. 69, 3092-3099 (2001).
  4. Gerdts, V., Uwiera, R. R. E., Mutwiri, G. K., Wilson, D. J., Bowersock, T., Kindane, A., Babiuk, L. A., Griebel, P. J. Multiple intestinal ‘loops’ provide an in vivo model to analyse multiple mucosal immune responses. J. Immunol. Methods. 256, 19-33 (2001).
  5. Greibel, P. J., Davis, W. C., Reynolds, J. D. An analysis of the growth and differentiation of b cells isolated from follicles from ileal Peyer’s patch of sheep. Immunology. 75, 601-607 (1992).
  6. Motyka, G., Greibel, P. J., Reynolds, J. D. Agents that activate protein kinase C resue sheep ileal Peyer’s patch B cells from apoptosis. Eur. J. Immunol. 23, 1314-1321 (1993).
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Cite This Article
Uwiera, R. R. E., Kastelic, J. P., Inglis, G. D. Catheterization of Intestinal Loops in Ruminants. J. Vis. Exp. (28), e1301, doi:10.3791/1301 (2009).

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